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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874586Generated: October 27, 2026

Methanol → Benzo[d]isoxazol-3-ylmethanol

https://huagongshe.com/reaction/874586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl 1,2-benzoxazole-3-carboxylateHCID 14177940—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductBenzo[d]isoxazol-3-ylmethanolHCID 5348746140.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

589 mg (3.0 mmol) of ethyl 1,2-benzoisoxazole-3-carboxylate in solution in 10 ml of tetrahydrofuran are added to a suspension of 129 mg (3.5 mmol) of lithium aluminum hydride in 5 ml of tetrahydrofuran. The reaction mixture is stirred for one hour at 60° C. and then treated by adding 2 ml of methanol dropwise, filtered through celite and rinsed with ethyl acetate. The organic phases are combined, dried over sodium sulfate and evaporated. The residue obtained is purified by chromatography on silica gel, elution being carried out with a 60/40 heptane/ethyl acetate mixture. 180 mg (39%) of benzoisoxazol-3-ylmethanol are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-cabbad3f9ab44ba68361859a0ef1b851
Source noteuspto-grants-2015_03